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Procalcitonin and C-Reactive Protein in the Diagnosis of Spontaneous Bacterial Peritonitis

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Procalcitonin and C-Reactive Protein in the Diagnosis of Spontaneous Bacterial Peritonitis 10 Original Article Procalcitonin and C-reactive protein in the diagnosis of spontaneous bacterial peritonitis Rajanshu Verma1, Sanjaya K. Satapathy2,3, Muhammad Bilal4 1Transplant Hepatology/Gastroenterology fellow, University of Tennessee Health Sciences Center, Memphis, TN, USA; 2Department of Transplant Surgery, Methodist University Hospital Transplant Institute/University of Tennessee Health Sciences Center, Memphis, TN, USA; 3Medical Director of Liver Transplantation, Division of Hepatology, Sandra Atlas Bass Center for Liver Diseases and Liver Transplantation, Northwell Health/North Shore University Hospital, Manhasset, New York, USA; 4Department of Gastroenterology, University of Tennessee Health Sciences Center, Memphis, Tennessee, USA Contributions: (I) Conception and design: M Bilal; (II) Administrative support: SK Satapathy, M Bilal; (III) Provision of study materials or patients: M Bilal; (IV) Collection and assembly of data: M Bilal, R Verma; (V) Data analysis and interpretation: R Verma, SK Satapathy; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors. Correspondence to: Muhammad Bilal, MD. Department of Gastroenterology, University of Tennessee Health Sciences Center, Memphis, Tennessee, USA. Email: [email protected]. Background: Spontaneous bacterial peritonitis (SBP) is a serious complication of cirrhosis and is associated with high morbidity and mortality. Rapid institution of appropriate antibiotics is central to the improved patient outcome. Correctly obtaining ascites fluid for analysis has several technical and logistic limitations resulting in overuse of empiric antibiotics when patients are admitted to the hospital with suspected SBP. Procalcitonin and C-reactive protein (CRP) are non-invasive markers of infection. We conducted a study to illustrate the role of these markers in making the diagnosis of SBP in patients with cirrhosis. Methods: A total of 45 patients were enrolled in this prospective cohort study, 14 (31.1%) of which were found to have SBP. Ascitic fluid neutrophils, serum procalcitonin and CRP levels were measured prior to initiation of antibiotics and these parameters were compared between the two groups. Area Under Receiver Operator Characteristic (AUROC) curves were used to assess the diagnostic accuracy of procalcitonin and CRP in this population. We defined neutrocytic SBP group as a combination of patients who had classic SBP (positive ascitic culture and >250 neutrophils/mm3) and culture-negative neutrocytic ascites. Results: Serum procalcitonin (2.81±2.59 vs. 0.43±0.48 ng/mL; P=0.0032), serum CRP (60.30±44.48 vs. 22.2±23.28; P=0.0055) and ascitic fluid neutrophil levels (49.23±30.90 vs. 16.7±20.39; P=0.0064) were significantly higher in SBP group than non-SBP group. AUROC for procalcitonin (cut-off >2.0 ng/mL) was 0.75 (95% CI, 0.61–0.88), CRP (cut-off >3.0 mg/L) was 0.55 (95% CI, 0.43–0.68) and for procalcitonin combined with CRP was 0.76 (95% CI, 0.61–0.90) for diagnosing all-cause SBP. In a subgroup analysis of patients with neutrocytic SBP, AUROC for procalcitonin was 0.88 (95% CI, 0.74–1.00), CRP was 0.62 (95% CI, 0.45–0.79) and for procalcitonin combined with CRP was 0.93 (95% CI, 0.81–1.00). Addition of CRP to procalcitonin did not significantly change the AUROC for diagnosis of SBP. Conclusions: Serum procalcitonin could be used as an adjunctive non-invasive biomarker in diagnosing SBP with a high degree of accuracy in cirrhotic patients. Addition of CRP does not seem to significantly increase the diagnostic accuracy of procalcitonin. Keywords: Procalcitonin; peritonitis; liver cirrhosis; C-reactive protein (CRP); diagnosis Received: 22 November 2020. Accepted: 12 May 2020. doi: 10.21037/tgh-19-297 View this article at: http://dx.doi.org/10.21037/tgh-19-297 © Translational Gastroenterology and Hepatology. All rights reserved. Transl Gastroenterol Hepatol 2020 | http://dx.doi.org/10.21037/tgh-19-297 Page 2 of 10 Translational Gastroenterology and Hepatology, 2020 Introduction To the best of our knowledge, ours is the first prospective study from United States describing the role Spontaneous bacterial peritonitis (SBP) is one of the of procalcitonin alone or in combination with CRP in turning points in the natural history of progression of diagnosing patients with SBP while adding to the growing cirrhosis which heralds the onset of decompensated disease. body of evidence that non-invasive markers may have a role It is associated with a high incidence of morbidity and in the diagnosis of this entity. mortality (up to 20–30%) as it puts cirrhotic patients at risk We aimed to assess the efficacy of serum procalcitonin of developing hepatic encephalopathy, renal failure, acidosis level and CRP in predicting the presence of SBP. and shock (1). Prompt initiation of antibiotics to treat SBP is the cornerstone of optimal therapy as it improves patient outcomes and survival (2). Primary prophylaxis Methods with antibiotics should be instituted in high-risk patients Patient selection (e.g., cirrhotics with low protein ascites, gastrointestinal hemorrhage) and secondary prophylaxis for those with a This was a prospective cohort study where cirrhotic patients prior history of SBP (3,4). with suspected SBP admitted to Methodist University Practice guidelines from various medical societies Hospital in Memphis, Tennessee, USA between September recommend doing a paracentesis in order to make a 2012 and March 2013 were consecutively enrolled in the diagnosis of SBP based on ascitic fluid neutrophil count study. The study was conducted in accordance with the prior to initiation of antibiotics (5,6). Given that the process Declaration of Helsinki (as revised in 2013) and approved of paracentesis requires skill, expertise in specimen handling by The Institutional Review Board of Methodist University and time delay associated with obtaining ascitic fluid cell Hospital, Memphis, Tennessee, USA (IRB approval count, many physicians in busy office practices in the number: 12-02006-XP). United States initiate antibiotics based on clinical suspicion All subjects in the study met the following inclusion alone which adds to the problem of growing antibiotic criteria: (I) cirrhosis with ascites; (II) clinical suspicion of resistance from overuse of unwarranted antibiotics. SBP, based at the minimum on: large volume ascites and Alternatively, the diagnosis of SBP can be entirely missed if new abdominal pain; (III) ascitic fluid WBC count and clinical suspicion is low and paracentesis is overlooked. In culture obtained before the use of antibiotics at admission high volume emergency rooms and busy outpatient clinics serum PCT and CRP measurements; (IV) absence of throughout the country, availability of a quick, reliable, infection in other organs or sites or those already on non-invasive marker for SBP would help crucial decision- antibiotics. making regarding need for paracentesis and promote appropriate antibiotic use. Paracentesis and procalcitonin, CRP estimation Procalcitonin (PCT), which is widely used as a marker of bacterial infection in various clinical conditions (e.g., We developed a protocol, at the Methodist University pneumonia, meningitis, bacterial gastroenteritis, septic Hospital Transplant Institute, for the measurement of serum shock) has also been studied in the setting of SBP and has procalcitonin (normal range: 0.5–2.0 ng/mL) and serum been found to accurately predict the presence of SBP when CRP (normal range: 0.5–3.0 mg/L) at the time of hospital present at elevated levels (7-17) (Table 1). Procalcitonin admission, prior to administering antibiotics. At our center, has been studied alone or in combination with other paracentesis is performed using aseptic technique and ascitic inflammatory markers such as TNF-alpha, IL-6, lipocalin/ fluid is inoculated into aerobic and anaerobic blood culture NGAL, MIP-1 beta and has been shown to be a sensitive bottles at bedside routinely. Fluid specimen is then sent off and specific marker for the diagnosis of SBP (7,13,18) promptly (within 1 hour) to the laboratory for ascitic fluid (Table 1). Similarly, CRP which is an acute phase reactant analysis. too has been found to be elevated in patients with SBP (19- Ascitic fluid (AF) was collected from hospitalized 21). CRP is a chemokine which is secreted by liver and can patients using sterile method and cultured in blood culture be elevated in a wide variety of clinical conditions including bottles, according to the guidelines of the Infectious infection, connective tissue disorders, malignancies and Diseases Society of America. Bacterial identification and autoimmune conditions. antimicrobial susceptibility testing were carried out as © Translational Gastroenterology and Hepatology. All rights reserved. Transl Gastroenterol Hepatol 2020 | http://dx.doi.org/10.21037/tgh-19-297 Translational Gastroenterology and Hepatology, 2020 Page 3 of 10 Table 1 Studies examining the role of serum procalcitonin in diagnosis of SBP Procalcitonin Cut-off value Author, year, country # of patients Underlying disease Sensitivity Specificity testing method (ng/mL) Viallon et al. (in 2000), France 61 Cirrhosis LUMItest 0.75 95% 98% Spahr et al. (in 2001), Switzerland 20 Cirrhosis LUMItest 0.5 50% 90% Connert et al. (in 2003), Germany 100 Cirrhosis LUMItest 0.58 92% 78% Yuan et al. (in 2013), China 84 Hepatitis B Diasorin 0.48 95% 79% Cekin et al. (in 2013), Turkey 101 Cirrhosis – 0.42 78% 75% Wu J et al. (in 2014), China 362 Cirrhosis – 0.462 83.7% 94.9% Lesinska et al. (in 2014), Poland 32 Cirrhosis LUMItest – – – Gharabaghi et al. (in 2015), Iran 33 Cirrhosis – 0.5 75% 92% Cai et al. (in 2015), China 78 Cirrhosis ELFA VIDAS 2.0 68.8% 94.2% Wu H et al. (in 2016), China 88 Cirrhosis ECLIA Cobas 0.78 77.5% 60.4% Abdel-Razik et al. (in 2016), Egypt 79 Cirrhosis ELISA RayBio 0.94 94.3% 91.8% SBP, spontaneous bacterial peritonitis. Table 2 Spontaneous bacterial peritonitis and its variants included classic SBP and CNNA. SBP types PMN ≥250 μL Culture Etiology of cirrhosis was recorded with respect to Classic SBP + + HBV, HCV, alcoholic, autoimmune cirrhosis and other conditions.
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